Canonical Allele Identifier: CA1694330835

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165977T= , CM000669.2:g.23165977T=	GRCh38
NC_000007.13:g.23205596T= , CM000669.1:g.23205596T=	GRCh37
NC_000007.12:g.23172121T=	NCBI36
NG_016983.1:g.65244T=
NG_016983.2:g.65244T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+39T= MANE Select	ENSP00000343273.4:n.1177+39T=
ENST00000339077.9:c.1177+39T=	ENSP00000343273.4:n.1177+39T=
ENST00000409689.5:c.1033+39T=	ENSP00000386263.1:n.1033+39T=
ENST00000469576.1:n.64+39T=
ENST00000521082.5:c.*1185+39T=	ENSP00000430351.1:n.*1185+39T=
NM_001031710.2:c.1177+39T=	NP_001026880.2:n.1177+39T=
NM_018846.4:c.1033+39T=	NP_061334.4:n.1033+39T=
NR_033328.1:n.1601+39T=
XM_006715753.1:c.1216+39T=	XP_006715816.1:n.1216+39T=
XM_006715754.1:c.1150+39T=	XP_006715817.1:n.1150+39T=
XM_006715755.1:c.1150+39T=	XP_006715818.1:n.1150+39T=
XM_006715756.1:c.1072+39T=	XP_006715819.1:n.1072+39T=
XM_006715753.3:c.1216+39T=	XP_006715816.1:n.1216+39T=
XM_006715754.3:c.1150+39T=	XP_006715817.1:n.1150+39T=
XM_006715755.3:c.1150+39T=	XP_006715818.1:n.1150+39T=
XM_006715756.3:c.1072+39T=	XP_006715819.1:n.1072+39T=
XM_017012439.2:c.1111+39T=	XP_016867928.1:n.1111+39T=
NM_001031710.3:c.1177+39T= MANE Select	NP_001026880.2:n.1177+39T=
NM_018846.5:c.1033+39T=	NP_061334.4:n.1033+39T=
NR_033328.2:n.1550+39T=